Non-specific interstitial pneumonia

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Non-specific interstitial pneumonia

Non-specific interstitial pneumonia (also known as Non-specific interstitial pneumonitis) (NSIP) is a form of idiopathic interstitial pneumonia.

Coding[1][edit]

ICD-9 ICD-10
516.32 J84.113 Idiopathic non-specific interstitial pneumonitis
516.33 J84.114 Acute interstitial pneumonitis

Symptoms[edit]

Symptoms include cough, difficulty breathing, and fatigue.[2]

Causes[edit]

It has been suggested that idiopathic nonspecific interstitial pneumonia has an autoimmune mechanism, and is a possible complication of undifferentiated connective tissue disease[3], however not enough research has been done at this time to find a cause. Patients with NSIP will often have other unrelated lung diseases like COPD or emphysema, along with other auto-immune disorders.

Diagnosis[edit]

A full clinical diagnosis can only be made from a lung biopsy of the tissue, fully best performed by a VATS, done by a cardio-thoracic surgeon. Some pulmonologists may first attempt a bronchoscopy, however this frequently fails to give a full or correct diagnosis.

Lung biopsies performed on patients with NSIP reveal two different disease patterns - cellular and fibrosing - which are associated with different prognoses. The cellular pattern displays chronic inflammation with minimal fibrosis. The fibrosing pattern displays interstitial fibrosis with various inflammation levels. Both patterns are uniform and lack the prominent fibroblastic foci that are found in other types of idiopathic interstitial pneumonia.[4]

Treatment[edit]

Commonly used drugs include prednisone, imuran, and cellcept. For active cases of pneumonia for these patients, Levaquin is a commonly used antibiotic. Almost all patients with NSIP will be on oxygen.

Prognosis[edit]

The fibrosing pattern of NSIP has a five year survival rate of 86% to 92%, while the cellular pattern of NSIP has a 100% five year survival rate. Patients with NSIP(whether cellular or fibrosing), have a better prognosis than those with usual interstitial pneumonia (UIP).[5]

References[edit]

  1. ^ "Convert ICD-9-CM Diagnosis 516.33 to ICD-10-CM". www.icd10data.com. Retrieved 2018-05-08. 
  2. ^ Cottin, V; Donsbeck, AV; Revel, D; Loire, R; Cordier, JF (October 1998). "Nonspecific interstitial pneumonia. Individualization of a clinicopathologic entity in a series of 12 patients". American Journal of Respiratory and Critical Care Medicine. 158 (4): 1286–93. doi:10.1164/ajrccm.158.4.9802119. PMID 9769293. 
  3. ^ Kinder, Brent W.; Collard, Harold R.; Koth, Laura; Daikh, David I.; Wolters, Paul J.; Elicker, Brett; Jones, Kirk D.; King, Talmadge E. (October 2007). "Idiopathic Nonspecific Interstitial Pneumonia". American Journal of Respiratory and Critical Care Medicine. 176 (7): 691–697. doi:10.1164/rccm.200702-220OC. PMC 1994238Freely accessible. PMID 17556720. 
  4. ^ Travis, William D.; Hunninghake, Gary; King, Talmadge E.; Lynch, David A.; Colby, Thomas V.; Galvin, Jeffrey R.; Brown, Kevin K.; Chung, Man Pyo; Cordier, Jean-François; du Bois, Roland M.; Flaherty, Kevin R.; Franks, Teri J.; Hansell, David M.; Hartman, Thomas E.; Kazerooni, Ella A.; Kim, Dong Soon; Kitaichi, Masanori; Koyama, Takashi; Martinez, Fernando J.; Nagai, Sonoko; Midthun, David E.; Müller, Nestor L.; Nicholson, Andrew G.; Raghu, Ganesh; Selman, Moisés; Wells, Athol (15 June 2008). "Idiopathic Nonspecific Interstitial Pneumonia". American Journal of Respiratory and Critical Care Medicine. 177 (12): 1338–1347. doi:10.1164/rccm.200611-1685OC. PMID 18388353. 
  5. ^ Travis, William D.; Matsui, Kazuhiro; Moss, Joel; Ferrans, Victor J. (January 2000). "Idiopathic Nonspecific Interstitial Pneumonia: Prognostic Significance of Cellular and Fibrosing Patterns". The American Journal of Surgical Pathology. 24 (1): 19. doi:10.1097/00000478-200001000-00003. PMID 10632484. 

External links[edit]

Classification
External resources